Issue 12, 1985

The acid-catalysed hydrolysis of O-methyl dimethylthiophosphinate. Direct evidence for pentaco-ordinate intermediate formation in the conversion of the P[double bond, length half m-dash]S ester into the P[double bond, length half m-dash]O ester

Abstract

Hydrolysis of the title compound in strong acid leads not only to the phosphinic acid but also to methyl dimethylphosphinate which could only be formed by the intermediacy of a pentaco-ordinate species.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 832-833

The acid-catalysed hydrolysis of O-methyl dimethylthiophosphinate. Direct evidence for pentaco-ordinate intermediate formation in the conversion of the P[double bond, length half m-dash]S ester into the P[double bond, length half m-dash]O ester

R. D. Cook and M. Metni, J. Chem. Soc., Chem. Commun., 1985, 832 DOI: 10.1039/C39850000832

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